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Pai syndrome: a review.
Olivero F, Foiadelli T, Luzzi S, Marseglia GL, Savasta S. Olivero F, et al. Childs Nerv Syst. 2020 Nov;36(11):2635-2640. doi: 10.1007/s00381-020-04788-z. Epub 2020 Jul 10. Childs Nerv Syst. 2020. PMID: 32651596 Free PMC article. Review.
BACKGROUND: Pai syndrome is a rare idiopathic developmental condition characterized by midline craniofacial abnormalities. ...OBJECTIVE: The aim of this review was to analyze the available evidence regarding Pai syndrome in order to better delineate th …
BACKGROUND: Pai syndrome is a rare idiopathic developmental condition characterized by midline craniofacial abnormalities. ... …
Nasal and lip polyps: Pai syndrome.
Pérez CG, Carrera Fernández S, Rodríguez D'Aquila A. Pérez CG, et al. Acta Otorrinolaringol Esp (Engl Ed). 2020 May-Jun;71(3):195-196. doi: 10.1016/j.otorri.2019.02.006. Epub 2019 Jun 10. Acta Otorrinolaringol Esp (Engl Ed). 2020. PMID: 31196564 English, Spanish. No abstract available.
Toward clinical and molecular dissection of frontonasal dysplasia with facial skin polyps: From Pai syndrome to differential diagnosis through a series of 27 patients.
Lehalle D, Bruel AL, Vitobello A, Denommé-Pichon AS, Duffourd Y, Assoum M, Amiel J, Baujat G, Bessieres B, Bigoni S, Burglen L, Captier G, Dard R, Edery P, Fortunato F, Geneviève D, Goldenberg A, Guibaud L, Héron D, Holder-Espinasse M, Lederer D, Lopez Grondona F, Grotto S, Marlin S, Nadeau G, Picard A, Rossi M, Roume J, Sanlaville D, Saugier-Veber P, Triau S, Valenzuela Palafoll MI, Vanlerberghe C, Van Maldergem L, Vezain M, Vincent-Delorme C, Zivi E, Thevenon J, Vabres P, Thauvin-Robinet C, Callier P, Faivre L. Lehalle D, et al. Am J Med Genet A. 2022 Jul;188(7):2036-2047. doi: 10.1002/ajmg.a.62739. Epub 2022 Apr 21. Am J Med Genet A. 2022. PMID: 35445792 Review.
Unique or multiple congenital facial skin polyps are features of several rare syndromes, from the most well-known Pai syndrome (PS), to the less recognized oculoauriculofrontonasal syndrome (OAFNS), encephalocraniocutaneous lipomatosis (ECCL), or Sakoda complex (SC) …
Unique or multiple congenital facial skin polyps are features of several rare syndromes, from the most well-known Pai syndrome …
Posterior impingement syndromes of the ankle.
Lee JC, Calder JD, Healy JC. Lee JC, et al. Semin Musculoskelet Radiol. 2008 Jun;12(2):154-69. doi: 10.1055/s-2008-1078703. Semin Musculoskelet Radiol. 2008. PMID: 18509795 Review.
Acute, or repetitive, compression of the posterior structures of the ankle may lead to posterior ankle impingement (PAI) syndrome, posteromedial ankle impingement (PoMI) syndrome, or Haglund's syndrome. ...The presence of an os trigonum or Stieda process is classica …
Acute, or repetitive, compression of the posterior structures of the ankle may lead to posterior ankle impingement (PAI) syndrome …
First Report of Pai Syndrome With Upper Alveolar Cavernous Hemangioma: Diagnosis and Surgical Treatment.
Demir CI, Yaşar EK, Bayrak BY, Işik H, Alagöz MŞ. Demir CI, et al. J Craniofac Surg. 2021 Jan-Feb 01;32(1):e31-e32. doi: 10.1097/SCS.0000000000006845. J Craniofac Surg. 2021. PMID: 32796311
This case describes the surgical methodology and the procedure for follow-up in a patient who had midline cleft of the upper lip, mid-alveolar cleft, double frenulum, and alveolar mass. Our patient is the first who meets the criteria for Pai syndrome with cavernous …
This case describes the surgical methodology and the procedure for follow-up in a patient who had midline cleft of the upper lip, mid-alveol …
Pai syndrome: challenging prenatal diagnosis and management.
Blouet M, Belloy F, Jeanne-Pasquier C, Leporrier N, Benoist G. Blouet M, et al. Pediatr Radiol. 2014 Sep;44(9):1184-7. doi: 10.1007/s00247-014-2966-4. Epub 2014 Apr 20. Pediatr Radiol. 2014. PMID: 24748063
Pai syndrome is a rare disorder that includes midline cleft lip, pericallosal lipoma and cutaneous polyp of the face. ...We emphasize the importance of facial examination with prenatal association of midline cleft lip and pericallosal lipoma in making the diagnosis …
Pai syndrome is a rare disorder that includes midline cleft lip, pericallosal lipoma and cutaneous polyp of the face. ...We em …
Diagnostic criteria in Pai syndrome: results of a case series and a literature review.
Morice A, Galliani E, Amiel J, Rachwalski M, Neiva C, Thauvin-Robinet C, Vazquez MP, Picard A, Kadlub N. Morice A, et al. Int J Oral Maxillofac Surg. 2019 Mar;48(3):283-290. doi: 10.1016/j.ijom.2018.08.010. Epub 2018 Sep 6. Int J Oral Maxillofac Surg. 2019. PMID: 30195458 Review.
Pai syndrome was originally described as the association of a midline cleft lip, midline facial polyps, and lipoma of the central nervous system. ...The study cohort consisted of seven case patients and an additional 60 cases diagnosed with Pai syndrome …
Pai syndrome was originally described as the association of a midline cleft lip, midline facial polyps, and lipoma of the cent …
Prenatal diagnosis of pericallosal lipoma: Systematic review.
Joigneau Prieto L, Ruiz Y, Pérez R, De León Luis J. Joigneau Prieto L, et al. Eur J Paediatr Neurol. 2019 Nov;23(6):764-782. doi: 10.1016/j.ejpn.2019.09.009. Epub 2019 Sep 25. Eur J Paediatr Neurol. 2019. PMID: 31587959

There was agenesis (partial or complete) of corpus callosum in 76.5% of the cases of tubulonodular lipoma and 8.3% of the cases of curvilinear lipoma (p < 0.001). There were three cases of Pai syndrome, and three cases of Goldenhar syndrome. Mean post-natal follo

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There was agenesis (partial or complete) of corpus callosum in 76.5% of the cases of tubulonodular lipoma and 8.3% of the cases of curviline …
Pai syndrome: a report of a case and review of the literature.
Al-Mazrou KA, Al-Rekabi A, Alorainy IA, Al-Kharfi T, Al-Serhani AM. Al-Mazrou KA, et al. Int J Pediatr Otorhinolaryngol. 2001 Nov 1;61(2):149-53. doi: 10.1016/s0165-5876(01)00555-9. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11589982 Review.
Pai syndrome is a rare congenital disorder first described in 1987. ...Full description of the clinico-pathological features and a review of the relevant medical literature is presented. To the best of our knowledge, this is the first case of Pai syndrome …
Pai syndrome is a rare congenital disorder first described in 1987. ...Full description of the clinico-pathological features a …
Atypical findings in three patients with Pai syndrome and literature review.
Lederer D, Wilson B, Lefesvre P, Poorten VV, Kirkham N, Mitra D, Verellen-Dumoulin C, Devriendt K. Lederer D, et al. Am J Med Genet A. 2012 Nov;158A(11):2899-904. doi: 10.1002/ajmg.a.35592. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987662 Review.
Pai syndrome is a rare disorder characterized by congenital nasal or facial polyp, midline cleft lip, pericallosal lipoma, ocular anomalies, and normal neuropsychological development. ...Thirty-three cases of Pai syndrome have been described so far. We …
Pai syndrome is a rare disorder characterized by congenital nasal or facial polyp, midline cleft lip, pericallosal lipoma, ocu …
24 results